Product Details

SNP ID

rs183796584

Assay Type

Functionally tested

NCBI dbSNP Submissions

9

Location

Chr.1:157125614 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAATGGGGACATTAAGGACACCTC[C/T]GCGGCCAGGGATTGGAGAGACAGCG

Phenotype

MIM: 164873

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CYCSP52 PubMed Links

Gene Details

Gene

CYCSP52

Gene Name

cytochrome c, somatic pseudogene 52

There are no transcripts associated with this gene.

Gene

ETV3

Gene Name

ETS variant 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145312.1	1055	Missense Mutation	AGA,GGA	R256G	NP_001138784.1
NM_005240.1	1055	Intron			NP_005231.1
XM_006711210.2	1055	Missense Mutation	AGA,GGA	R256G	XP_006711273.1

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